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Titel:

Loss-of-Function Variants in HOPS Complex Genes VPS16 and VPS41 Cause Early Onset Dystonia Associated with Lysosomal Abnormalities.

Dokumenttyp:
Article; Journal Article; Research Support, Non-U.S. Gov't
Autor(en):
Steel, Dora; Zech, Michael; Zhao, Chen; Barwick, Katy E S; Burke, Derek; Demailly, Diane; Kumar, Kishore R; Zorzi, Giovanna; Nardocci, Nardo; Kaiyrzhanov, Rauan; Wagner, Matias; Iuso, Arcangela; Berutti, Riccardo; Škorvánek, Matej; Necpál, Ján; Davis, Ryan; Wiethoff, Sarah; Mankad, Kshitij; Sudhakar, Sniya; Ferrini, Arianna; Sharma, Suvasini; Kamsteeg, Erik-Jan; Tijssen, Marina A; Verschuuren, Corien; van Egmond, Martje E; Flowers, Joanna M; McEntagart, Meriel; Tucci, Arianna; Coubes, Philippe;...     »
Abstract:
OBJECTIVES: The majority of people with suspected genetic dystonia remain undiagnosed after maximal investigation, implying that a number of causative genes have not yet been recognized. We aimed to investigate this paucity of diagnoses. METHODS: We undertook weighted burden analysis of whole-exome sequencing (WES) data from 138 individuals with unresolved generalized dystonia of suspected genetic etiology, followed by additional case-finding from international databases, first for the gene impl...     »
Zeitschriftentitel:
Ann Neurol
Jahr:
2020
Band / Volume:
88
Heft / Issue:
5
Seitenangaben Beitrag:
867-877
Volltext / DOI:
doi:10.1002/ana.25879
PubMed:
http://view.ncbi.nlm.nih.gov/pubmed/32808683
Print-ISSN:
0364-5134
TUM Einrichtung:
617; Institut für Humangenetik; Lehrstuhl für Neurogenetik (Prof. Winkelmann)
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